Canonical Allele Identifier: CA7813542

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1526004C>T , CM000678.2:g.1526004C>T	GRCh38
NC_000016.9:g.1576005C>T , CM000678.1:g.1576005C>T	GRCh37
NC_000016.8:g.1516006C>T	NCBI36
NG_032783.1:g.91105G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014714.4:c.2651G>A MANE Select	NP_055529.2:p.Arg884Gln
ENST00000426508.7:c.2651G>A MANE Select	ENSP00000406012.2:p.Arg884Gln
NM_014714.3:c.2651G>A	NP_055529.2:p.Arg884Gln
ENST00000361339.9:c.233G>A	ENSP00000354895.5:p.Arg78Gln
ENST00000397417.6:c.*1089G>A	ENSP00000380562.2:n.*1089G>A
ENST00000426508.6:c.2651G>A	ENSP00000406012.2:p.Arg884Gln
ENST00000565298.5:n.1880G>A
ENST00000566818.1:n.366G>A
XM_006720989.2:c.2651G>A	XP_006721052.1:p.Arg884Gln
XM_006720990.2:c.2651G>A	XP_006721053.1:p.Arg884Gln
XM_006720990.3:c.2651G>A	XP_006721053.1:p.Arg884Gln
XM_006720991.2:c.2651G>A	XP_006721054.1:p.Arg884Gln
XM_006720991.3:c.2651G>A	XP_006721054.1:p.Arg884Gln
XM_006720992.2:c.284G>A	XP_006721055.1:p.Arg95Gln
XM_006720992.3:c.284G>A	XP_006721055.1:p.Arg95Gln
XM_011522766.1:c.2405G>A	XP_011521068.1:p.Arg802Gln
XM_011522766.3:c.2405G>A	XP_011521068.1:p.Arg802Gln
XM_011522767.1:c.1676G>A	XP_011521069.1:p.Arg559Gln
XM_011522767.2:c.1676G>A	XP_011521069.1:p.Arg559Gln
XM_017023910.1:c.2651G>A	XP_016879399.1:p.Arg884Gln
XM_017023911.1:c.836G>A	XP_016879400.1:p.Arg279Gln